{"product_id":"amelogenesis-dentinogenesis-imperfecta-panel-por-exoma-clinico-sec-cnvs-38-genes","title":"AMELOGENESIS\/DENTINOGENESIS IMPERFECTA: CLINICAL EXOME PANEL (Sec. \u0026amp; CNVs) – 38 genes","description":"\u003cp\u003eIt evaluates inherited enamel and dentin disorders with hypoplasia\/hypomaturation, brittle teeth, discoloration, sensitivity, and early tooth loss, both isolated and syndromic (e.g., osteogenesis imperfecta). It allows for precise molecular identification and planning of restoration, prevention, and systemic follow-up. Genes analyzed: AMELX, ENAM, FAM83H, MMP20, KLK4, WDR72, DSPP, COL1A1, COL1A2, LAMB3, and others. You can consult the complete list of analyzed genes by contacting Genotica.\u003c\/p\u003e","brand":"LabGenetics","offers":[{"title":"Default Title","offer_id":52131418767626,"sku":null,"price":850.0,"currency_code":"EUR","in_stock":true}],"url":"https:\/\/www.genotica.com\/en\/products\/amelogenesis-dentinogenesis-imperfecta-panel-por-exoma-clinico-sec-cnvs-38-genes","provider":"Genotica","version":"1.0","type":"link"}